Session 7: Cystic Fibrosis and Bronchiectasis Flashcards

1
Q

What is cystic fibrosis?

A

Autosomal recessive disease leading to a mutation in CFTR. Multisystem disease with thickened secretions.

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2
Q

How to diagnose CF.

A

Phenotypic features like a history of CF or a positive new born screening result.

Also a sweat test to check for increased sweat chloride concentrations.

Can also be done by demonstration of abnormal nasal epithelial transport.

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3
Q

How may CF present in newborns?

A

Meconium ileus

Intestinal malabsorption

Recurrent chest infections

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4
Q

Explain meconium ileus as a presentation of CF.

A

CF infants bowel might be blocked by sticky secretions. Leading to intestinal obstruction, bilious vomiting, abdo distension and delay in passing meconium.

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5
Q

Why do infants with CF present with intestinal malabsorption?

A

Main cause is du to a severe deficiency of pancreatic enzymes.

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6
Q

Signs and symptoms of CF.

A

Chronic sinusitis.

Recurrent lower resp tract infections.

Finger clubbing

Abnormal sweat secretions

Male infertility

Gall stones, liver disease and portal hypertension.

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7
Q

Common CF complications.

A

Recurrent resp infections

Low body weight

Distal intestinal obstruction syndrome

CF related diabetes

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8
Q

Management of resp infections due to CF.

A

Aggressive therapy with physio and antibiotics.

Often receiving prophylactic antibiotics to maintain health.

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9
Q

Explain cause of low body weight in CF.

A

Consequence of pancreatic insufficiency leading to intestinal malabsorption.

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10
Q

Management of low body weight due to CF.

A

Pancreatic enzyme replacement therapy.

High calorie intake and often extra supplements.

NG or PEG feeding

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11
Q

What is distal intestinal obstruction syndrome? (DIOS)

A

Due to intestinal contents in the distal ileum and proximal colon which are thick and dehydrated.

Mainly due to no pancreatic enzymes, salt deficiency or hot weather.

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12
Q

What’s the difference between DIOS and constipation?

A

DIOS is a faecal obstruction in ileo-caecum.

Constipation is whole bowel.

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13
Q

How to diagnose DIOS.

A

Palpable right iliac fossa mass.

Abdo x-ray

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14
Q

Management of CF in general.

A

No smoking

Avoid other CF patients

Avoid people with infections

Avoid jacuzzies (pseudomonas)

Keep things clean

Avoid fungi

Immunisation for influenza

NaCl tablets

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15
Q

What is bronchiectasis?

A

Chronic dilation of one or more bronchi with poor mucus clearance of the bronchi and recurrent or chronic bacterial infections.

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16
Q

How to diagnose bronchiectasis.

A

High resolution CT

17
Q

Causes of bronchiectasis.

A

Whooping cough

TB

Hypogammaglobulinaemia

CF

Young’s syndrome

Kartagener syndrome

Obstruction of bronchi by foreign body, tumour or lymph node.

18
Q

What is Young’s syndrome?

A

A triad of bronchiectasis, sinusitis and reduced fertility.

19
Q

What is Kartagener syndrome?

A

Triad of bronchiectasis, sinusitis and situs inversus.

20
Q

Common organisms causing bronchiectasis.

A

Haemophilus influenzae

Pseudomonas aeruginosa

Moraxella catarrhalis

21
Q

Management of bronchiectasis.

A

Treat underlying cause.

Physiotherapy with mucus clearance

Antibiotics

Flu vaccine, bronchodilators

Pulmonary rehab

22
Q

What will a CT to diagnose bronchiectasis show?

A

Signet ring sign.

23
Q

Explain signet ring sign.

A

Dilated bronchus and accompanying pulmonary artery.

24
Q

Symptoms and signs of bronchiectasis.

A

Chronic cough

Daily sputum production

Breathlessness on exertion

Intermittent haemoptysis

Nasal symptoms

Chest pain

Fatigue

Wheezing (less common)

25
Q

What might you hear upon examination of bronchiectasis?

A

Fine crackles.

Rhonci

Wheezing

26
Q

Explain the function of CFTR.

A

Transports chloride and bicarbonate and regulates the ENaC.

Enables Cl’ to be transported out of cells into airways. This helps control the movement of water as well.

It also regulates the sodium reabsorption into cells.

This means that CFTR plays a major role in hydration of mucus at the surface of the airway track.

Defective CFTR leads to airway surface liquid dehydration.

This leads to sticky and thick mucous which impairs the muco-ciliary clearance.